A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392282



Internal ID21049835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53460477..53471753hg38UCSC Ensembl
chr4:54326644..54337920hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3811277
hg1911277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211918
Samples
Known GenesLNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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